Korean J Urol.  2006 Sep;47(9):1007-1012. 10.4111/kju.2006.47.9.1007.

Urethral Dysfunction in a Non-Insulin Dependent Diabetes Mellitus Rat Model

Affiliations
  • 1Department of Urology, Inha University College of Medicine, Incheon, Korea. lt11@inha.ac.kr

Abstract

Purpose
We assessed whether urethral dysfunction related to nitric oxide (NO) is responsible for voiding dysfunction in rats with non-insulin dependent diabetes mellitus.
Materials and Methods
A total of 27 male Sprague-Dawley rats (14 diabetic rats and 13 control rats) were included. Diabetes mellitus was induced by intraperitoneal administration of streptozotocin (90mg/kg) on the second day after birth. Cystometry with determining the detrusor leak point pressure (LPP) was performed in the diabetic and control rats at the age of 12 and 24 weeks. The effect of intravenous injection with L- nitro-arginine-methyl ester (L-NAME) as a NO inhibitor and sodium nitroprusside (SNP) as a NO donor were also evaluated.
Results
Diabetic rats showed an increased bladder capacity and a higher detrusor LPP than the controls at both ages. After intravenous injection of L-NAME, the control rats showed an increased detrusor LPP, but no change was observed in the diabetic rats. With administering SNP, the detrusor LPP was decreased in both the diabetic and control rats.
Conclusions
Urethral resistance was more increased in the diabetic rats than the controls, which may be the result of dysfunction of the urethral nerve containing NO. The urethral factor, in addition to cystopathy, also plays an important role for the pathogenesis of voiding dysfunction in diabetic patients.

Keyword

Diabetes mellitus; Urethra; Nitric oxide

MeSH Terms

Animals
Diabetes Mellitus*
Humans
Injections, Intravenous
Male
Models, Animal*
NG-Nitroarginine Methyl Ester
Nitric Oxide
Nitroprusside
Parturition
Rats*
Rats, Sprague-Dawley
Streptozocin
Tissue Donors
Urethra
Urinary Bladder
NG-Nitroarginine Methyl Ester
Nitric Oxide
Nitroprusside
Streptozocin

Figure

  • Fig. 1 Diagrammatic representation for defining the parameter (detrusor LPP) and the findings of cystometry. The upper part is the pressure tracing in the bladder and the lower is that in the urethra. The detrusor LPP is measured by the bladder pressure at which the stable urethral pressure abruptly rises. The findings are without medication (A), premedicated with L-NAME (B) and with sodium nitroprusside (C). LPP: leak point pressure.

  • Fig. 2 Trends of the glucose levels in diabetes-induced rats (the NIDDM model). Transient hyperglycemia rapidly developed that this lasted for 2-4 days. The plasma glucose concentrations remained at near normal levels until about 6 weeks of age, whereupon frank chronic hyperglycemia developed with plasma glucose concentrations that usually ranged between 200-500mg/dl.


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